rs879255396
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs879255396(A;C) |
Make rs879255396(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 113902864 |
Gene | AP4B1, DCLRE1B |
is a | snp |
is | mentioned by |
dbSNP | rs879255396 |
dbSNP (classic) | rs879255396 |
ClinGen | rs879255396 |
ebi | rs879255396 |
HLI | rs879255396 |
Exac | rs879255396 |
Gnomad | rs879255396 |
Varsome | rs879255396 |
LitVar | rs879255396 |
Map | rs879255396 |
PheGenI | rs879255396 |
Biobank | rs879255396 |
1000 genomes | rs879255396 |
hgdp | rs879255396 |
ensembl | rs879255396 |
geneview | rs879255396 |
scholar | rs879255396 |
rs879255396 | |
pharmgkb | rs879255396 |
gwascentral | rs879255396 |
openSNP | rs879255396 |
23andMe | rs879255396 |
SNPshot | rs879255396 |
SNPdbe | rs879255396 |
MSV3d | rs879255396 |
GWAS Ctlg | rs879255396 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255396(C;C) rs879255396(G;G) |
Alt | rs879255396(C;C) rs879255396(G;G) |
Reference | Rs879255396(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DCLRE1B AP4B1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.114445486T>G |
CLNSRC | |
CLNACC | RCV000239291.1, |